genomics

By coupling cell lineage tracking with molecular gene expression patterns, researchers deciphered how gene activity influences immune cell production.

Learn how cutting-edge sequencing techniques accelerate basic and disease research.

Used across a wide range of techniques and methods, water quality has a pivotal role in genetics and genomics research.

With nanoliter-scale reaction volumes, microfluidics-based real-time PCR (RT-PCR) devices speed up genomic analyses and library prep.

A novel platform paves the way for genomics-based oncology testing, with a knowledgebase of actionable biomarkers and help for scientists developing in-house tests.

Molecular studies may point to underlying genetics and therapeutic targets.

Comparing mammoth and elephant genomes revealed genetic mutations that may have helped mammoths survive in the Arctic.

In this webinar, Joshua Campbell will talk about the fundamentals of scRNA-seq analysis and how to handle various challenges. 

Next generation sequencing (NGS) core facility scientists and researchers discuss their latest work exploring novel cancer models and stem cells in space.

Neurobiologists, computer scientists, and engineers join forces to grow mini brains using automation and make their technologies smarter with artificial intelligence.

Centralized core facilities and commercial service providers specializing in NGS provide expertise and training for researchers new to the method.

Learn how to successfully use next generation sequencing to gain valuable research insights with the expert help of core laboratories.

Next-generation sequencing (NGS) core facility scientists and researchers new to NGS discuss their fruitful collaborations, highlighting how to receive expert help from genomics facilities.

Lasker Award winner Evelyn Witkin discovered the mechanism for DNA repair following UV damage.

By studying the genomes of more than 24,000 individuals, researchers discovered rare genetic mutations that may shed light on mechanisms underlying schizophrenia.

Multiomics combines multiple layers of biology to power new discoveries in disease research. 

A conversation with Illumina Distinguished Scientist and Vice President Gary Schroth about the present and future of multiomic technology and applications

Learn when to select absorbance or fluorescence to assess sample quantity and quality.

Researchers across disciplines combine layers of discovery obtained with accessible NGS-based multiomics approaches.

Correlated regions of systemic inter-individual epigenetic variation (CoRSIV) target-capture bisulfite sequencing allows researchers to identify disease-associated epigenetic variation.